6970-28-1

Basic information

• Product Name: (R)-2,4-Diaminobutyric acid dihydrochloride
• Synonyms: (R)-2,4-Diaminobutyricacid2HCl;(2R)-2,4-diazaniumylbutanoate;2,4-Diaminobutyric acid dihydrochloride
• CAS NO: 6970-28-1
• Molecular Formula: C₄H₁₀N₂O₂*2ClH
• Molecular Weight: 191.05628
• Mol File: 6970-28-1.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 321°C at 760 mmHg
• Flash Point: 147.9°C
• Appearance: /
• Density: 1.218g/cm³
• Vapor Pressure: 6.36E-05mmHg at 25°C
• Refractive Index: 1.513
• CAS DataBase Reference: (R)-2,4-Diaminobutyric acid dihydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-2,4-Diaminobutyric acid dihydrochloride(6970-28-1)
• EPA Substance Registry System: (R)-2,4-Diaminobutyric acid dihydrochloride(6970-28-1)

Safety Data

• Hazardous Substances Data: 6970-28-1(Hazardous Substances Data)

Usage

General Description

(R)-2,4-Diaminobutyric acid dihydrochloride is a chemical compound that is commonly used in research and pharmaceutical applications. It is an amino acid derivative with two amino groups and a carboxylic acid group, and it exists as a dihydrochloride salt in its chemical form. (R)-2,4-Diaminobutyric acid dihydrochloride has been studied for its potential as a therapeutic agent for conditions such as epilepsy and neurodegenerative diseases. It has also been investigated for its potential to enhance the function of neurotransmitter receptors in the brain. The dihydrochloride salt form of (R)-2,4-Diaminobutyric acid is water-soluble, making it suitable for use in aqueous solutions and biological systems. Overall, this compound has potential for various medical and research applications due to its unique chemical structure and biological activity.

InChI:InChI=1/C4H10N2O2/c5-2-1-3(6)4(7)8/h3H,1-2,5-6H2,(H,7,8)/t3-/m1/s1

Upstream product

• 103668-08-2 (R)-2,4-Diamino-butyric acid ethyl ester; hydrochloride 
• 34404-27-8 N^α,N^γ-bis(t-butoxycarbonyl)-L-α,γ-butyric acid 
• 127531-09-3 (S)-3-Cyano-2-[(1R,2R,5R)-2-hydroxy-2,6,6-trimethyl-bicyclo[3.1.1]hept-(3E)-ylideneamino]-propionic acid ethyl ester 

Downstream Products

• 95766-36-2 H-A₂bu(Z)-OH 
• 1217645-10-7 (R)-2,4-bis((((9H-fluoren-9-yl)methoxy)carbonyl)amino)butanoic acid 
• 55478-23-4 (S)-2,4-bis(((benzyloxy)carbonyl)amino)butanoic acid 
• 2483-65-0 3-amino-pyrrolidin-2-one 
• 4128-00-1 (3S)-3-aminopyrrolidin-2-one 
• 25139-87-1 ⁽⁵⁾-(+)(D)-N,N'-Ditosyl-2,4-diamino-butanol 
• 126581-98-4 DPAB-L-DBA (trans) 
• 117106-22-6 (S)-4-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-aminobutanoic acid 
• 97347-23-4 N^α,N^γ-diBoc-L-2,4-diaminobutyric acid p-nitrobenzyl ester 

Relevant articles and documents

Preparation of enantiopure 2-acylazetidines and their reactions with chloroformates

Enantiopure 1-phenylethylazetidine-2-carboxylates and 2-acylazetidines were prepared and reacted with chloroformates to yield α-chloro-γ-amino butyric acid esters and ketones from ring opening reaction of azetidinium ion intermediate in a completely regio- and stereoselective manner.